Canonical Allele Identifier: PA2825276943
Gene: CHEK2 HGNC NCBI

Linked Data

ClinVar Variation Id: 140932

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001005735.1:p.Ser295Asn
CA163957
NM_001005735.2:c.884G>A